Vitiligo-associated autoimmune disease
General Information (adopted from Orphanet):
Synonyms, Signs: |
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Number of Symptoms | 2 |
OrphanetNr: | 247871 |
OMIM Id: |
193200
606579 607836 608391 608392 609400 |
ICD-10: |
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UMLs: |
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MeSH: |
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MedDRA: |
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Snomed: |
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Prevalence, inheritance and age of onset:
Prevalence: | No data available. |
Inheritance: |
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Age of onset: |
Childhood Adolescent Adult [Orphanet] |
Disease classification (adopted from Orphanet):
Parent Diseases: |
Autoinflammatory syndrome with skin involvement
-Rare skin disease Mixed autoinflammatory and autoimmune syndrome -Rare systemic or rheumatologic disease |
Symptom Information:
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(HPO:0003764) | Nevus | 17 / 7739 | ||||
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(HPO:0001045) | Vitiligo | 13 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
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